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This is our deepest domain. We build connected medical devices, HL7 FHIR interoperability at scale, medical device software to IEC 62304, and clinical AI that runs at the edge with zero data egress. From secure-boot gateways and remote imaging control to air-gapped inference, we engineer to ISO 13485 discipline: traceable, verifiable and safe.
Clinical software touches patients, protected data and regulated workflows. It has to be traceable, interoperable and resilient when the network, the power or the cloud is not there.
ISO 13485*
the quality system we hold and build medical device software to.
Zero egress*
clinical AI that runs air-gapped, so protected data never leaves the device.
FHIR*
HL7 FHIR interoperability at millions of records per minute.
Reflecting our certified medical work and proven edge, imaging and interoperability delivery.
From the connected device to the clinical cloud, with the safety, security and interoperability the domain demands.
Software as a medical device and embedded firmware built to IEC 62304 lifecycle discipline, with traceable requirements, risk management and verification evidence an auditor accepts.
FHIR transformation and integration pipelines that move millions of records per minute on Kafka and GKE, so clinical data flows cleanly between systems without loss or ambiguity.
Connected device gateways with a hardware root of trust, secure boot and signed updates on Yocto, U-Boot and TPM, bridging device protocols to Azure IoT and the cloud.
On-device LLMs and RAG that run air-gapped with zero data egress, so inference happens at the point of care and protected health information never leaves the device.
Remote MRI and CT control, ophthalmology device simulators and DDS-to-Azure robotics gateways, built for the latency, safety and reliability that clinical hardware requires.
Secure cloud, data and application platforms with encryption, identity and audit trails aligned to HIPAA, so protected data is handled correctly end to end.
A verification-led path from a clinical requirement to a device or platform you can certify, trust and put in front of patients.
Capture clinical and regulatory requirements with traceability from the start, so every line maps back to an intent, a risk control and a test.
Architect for patient safety, data protection and resilience, with risk management and the verification strategy defined before code is written.
Structured testing, reviews and evidence capture under our ISO 13485 and IEC 62304 discipline, so the system does what the spec says and you can prove it.
Signed updates, monitoring and a documented, controlled baseline, so the device stays safe and compliant through its whole clinical life.
Capture clinical and regulatory requirements with traceability from the start, so every line maps back to an intent, a risk control and a test.
Architect for patient safety, data protection and resilience, with risk management and the verification strategy defined before code is written.
Structured testing, reviews and evidence capture under our ISO 13485 and IEC 62304 discipline, so the system does what the spec says and you can prove it.
Signed updates, monitoring and a documented, controlled baseline, so the device stays safe and compliant through its whole clinical life.
Connected, regulated and edge medical systems we have shipped in clinical and life sciences environments. Client names withheld under NDA.
We built a streaming FHIR transformation pipeline on Kafka and GKE that ingests, maps and normalizes clinical records at scale, so downstream systems receive clean, standards-compliant data without loss.
FHIR
HL7 standards-compliant
Millions/min
records transformed
Zero loss
clean end-to-end mapping
We delivered a connected medical gateway on Yocto, U-Boot and TPM with secure boot and signed over-the-air updates, bridging device protocols to Azure IoT so the device stays trustworthy through its whole life.
Secure boot
TPM root of trust
Signed
over-the-air updates
Azure IoT
cloud-connected
We deployed on-device LLMs with RAG on Ollama and Qdrant that run fully offline at the point of care, so protected health information never leaves the device and inference continues when the link does not.
Zero egress
data stays on-device
Air-gapped
runs fully offline
On-device
RAG at the edge
Standards and experience
Clinical software is not a matter of taste. We hold ISO 13485, design to IEC 62304 and HIPAA, and we back it with real connected-device, imaging and interoperability delivery.
Our experience
Secure-boot medical gateways, remote imaging control, FHIR at scale and air-gapped clinical AI, shipped into regulated healthcare and life sciences environments.
designed to
ISO 13485
Medical quality
Quality management for medical device design and manufacture, a certification we hold.
IEC 62304
Device software lifecycle
Lifecycle processes for medical device software, from requirements to maintenance.
HL7 FHIR
Interoperability
Standard for exchanging healthcare data cleanly between clinical systems.
HIPAA
Data protection
Safeguards for protected health information across storage, access and transit.
The result is medical software and devices that are traceable, interoperable and safe, and that hold up when a regulator or an auditor arrives.
Capabilities
Product Engineering
AI, Data & Intelligent Systems
UX & Product Design
Experience Engineering
Cybersecurity
Compliance Engineering
US · Muscat · Bangalore · Puttur, ISO 13485:2016 · ISO 27001:2013 · ISO 9001:2015
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